Background While commercial poultry and captive birds are exposed to antimicrobials through direct medication, environmental pollution may result in contamination of wild birds. Fluoroquinolones are commonly used medications to treat severe avian bacterial infections; however, their adverse effects on birds remain understudied. Here, we examine toxicity of enrofloxacin and marbofloxacin during the egg incubation period using the chicken ( Gallus Gallus domesticus ) as a model avian species. Laboratory tests were based on eggs injected with 1, 10 and 100 μg of fluoroquinolones per 1 g of egg weight prior to the start of incubation and monitoring of chick blood biochemistry, reproductive parameters and heart rate during incubation. Results Eggs treated with fluoroquinolones displayed reduced hatchability due to embryonic mortality, particularly on day 13 of incubation. Total hatching success showed a similar pattern, with a significantly reduced hatchability in low and high exposure groups treated with both enrofloxacin and marbofloxacin. From 15 to 67% of chicks hatching in these groups exhibited joint deformities. Hatching one-day pre-term occurred with a prevalence of 31 to 70% in all groups treated with fluoroquinolones. Embryonic heart rate, measured on days 13 and 19 of incubation, increased in all enrofloxacin-treated groups and medium and high dose groups of marbofloxacin-treated eggs. Blood biochemistry of chicks sampled at hatch from medium dose groups showed hypoproteinaemia, decreased uric acid and increased triglycerides. Chicks from the enrofloxacin-treated group displayed mild hyperglycaemia and a two-fold rise in the blood urea nitrogen to uric acid ratio. Principal components analysis based on blood biochemistry clearly separated the control bird cluster from both enrofloxacin- and marbofloxacin-treated birds. Conclusions Fluoroquinolones induce complex adverse effects on avian embryonic development, considerably reducing the performance of incubated eggs and hatching chicks. Cardiotoxicity, which quickens embryonic heart rate, meant that the total number of heart beats required for embryogenesis was achieved earlier than in the standard incubation period, resulting in pre-term hatching. Our data suggest that enrofloxacin has a higher potential for adverse effects than marbofloxacin. To conclude, care should be taken to prevent exposure of reproducing birds and their eggs to fluoroquinolones. Electronic supplementary material The online version of this article (10.1186/s12917-019-1957-y) contains supplementary material, which is available to authorized users.

Polychlorinated biphenyls (PCBs) are carcinogens causing endocrine disruption. While production of PCBs is now banned, wildlife exposure still occurs due to environmental contamination. We investigated thyroid toxicity in wild ungulates using three-dimensional primary thyrocyte cultures exposed to PCB 138 for 24, 48, and 72 h at concentrations ranging within 0–3000 ng/ml. Thyrocyte viability ranged within 78.71–118.34%, 98.14–104.45%, and 84.16–106.70% in fallow deer-, mouflon-, and roe deer-derived cells, respectively. Viability decreased significantly in fallow deer (P = 0.012) and roe deer (P = 0.002) thyrocytes exposed for 48 h at 30 ng/ml. While cytotoxicity ranged within 2.36–16.37%, 3.19–9.85%, and 2.76–11.21% in fallow deer, mouflon, and roe deer, respectively, only roe deer displayed significantly higher cytotoxicity at a 3 ng/ml exposure (P < 0.05) and lower cytotoxicity at 30 ng/ml (P < 0.01). Exposure to 30 ng/ml for 24 and 48 h induced reactive oxygen species in fallow deer. Iodide uptake at 30 ng/ml exposure increased after 24 h in fallow and roe deer, but showed a significant drop after 48 and 72 h in fallow deer, mouflon, and roe deer. Thyroxine T4 release at 30 ng/ml exposure decreased significantly after 48 and 72 h; 24, 48 and 72 h; and 48 h in fallow deer, mouflon, and roe deer, respectively. Our findings indicate time- and species-dependent effects of PCB on performance and thyrocyte function. Use of cell culture models reduces the number of experimental specimens, increases test species welfare and replaces whole organisms with specific target cells.

The greater mouse-eared bat ( Myotis myotis ) is a flagship species for the protection of hibernation and summer maternity roosts in the Western Palearctic region. A range of pathogenic agents is known to put pressure on populations, including the white-nose syndrome fungus, for which the species shows the highest prevalence and infection intensity of all European bat species. Here, we perform analysis of blood parameters characteristic for the species during its natural annual life cycle in order to establish reference values. Despite sexual dimorphism and some univariate differences, the overall multivariate pattern suggests low seasonal variation with homeostatic mechanisms effectively regulating haematology and blood biochemistry ranges. Overall, the species displayed a high haematocrit and haemoglobin content and high concentration of urea, while blood glucose levels in swarming and hibernating bats ranged from hypo- to normoglycaemic. Unlike blood pH, concentrations of electrolytes were wide ranging. To conclude, baseline data for blood physiology are a useful tool for providing suitable medical care in rescue centres, for studying population health in bats adapting to environmental change, and for understanding bat responses to stressors of conservation and/or zoonotic importance.

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As a surrogate for the whole organism, primary cultures and cell lines serve as valuable tools for investigating exogenous and endogenous cytopathy. Studying cell responsiveness to diseases and contaminants is considered a less demanding and more readily accessible research approach that minimizes animal distress and provides more specific data. In the current work, the authors established primary cultures from several different organs and tissues of common carp (Cyprinus carpio L.) for subsequent use in other applications. They investigated the technical challenges in obtaining successful and durable carp-derived tissue cultures. The trials indicate that the type of tissue grown, carp strain and fish age impact equally upon culturing success, as do the cultivating conditions. Cells from gill epithelia, head and trunk kidneys, spleen, skin, gonads and ocular tissue were successfully established and maintained for further use in in-vitro testing. The primary cultures were, therefore, used to investigate and assess pathogens and pollutants emerging in carp's environment.